Griffero, Mariana; Benedetti, Anna Flavia Figueredo; Perez, Marcela; Carvalho, Luciani; Jorge, Alexander Augusto de Lima 
; Xavier, Ana Claudia Latronico ; Mendonca, Berenice Bilharinho de ; Arnhold, Ivo; Mericq, Veronica
Fonte: Journal of pediatric endocrinology & metabolism. Unidade: FM
Assuntos: MUTAGÊNESE, DOENÇAS CONGÊNITAS, PEDIATRIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GRIFFERO, Mariana et al. Novel OTX2 loss of function variant associated with congenital hypopituitarism without eye abnormalities. Journal of pediatric endocrinology & metabolism, v. 35, n. 6, p. 831-835, 2022Tradução . . Disponível em: https://doi.org/10.1515/jpem-2021-0719. Acesso em: 12 nov. 2024.APA
Griffero, M., Benedetti, A. F. F., Perez, M., Carvalho, L., Jorge, A. A. de L., Xavier, A. C. L., et al. (2022). Novel OTX2 loss of function variant associated with congenital hypopituitarism without eye abnormalities. Journal of pediatric endocrinology & metabolism, 35( 6), 831-835. doi:10.1515/jpem-2021-0719NLM
Griffero M, Benedetti AFF, Perez M, Carvalho L, Jorge AA de L, Xavier ACL, Mendonca BB de, Arnhold I, Mericq V. Novel OTX2 loss of function variant associated with congenital hypopituitarism without eye abnormalities [Internet]. Journal of pediatric endocrinology & metabolism. 2022 ; 35( 6): 831-835.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1515/jpem-2021-0719Vancouver
Griffero M, Benedetti AFF, Perez M, Carvalho L, Jorge AA de L, Xavier ACL, Mendonca BB de, Arnhold I, Mericq V. Novel OTX2 loss of function variant associated with congenital hypopituitarism without eye abnormalities [Internet]. Journal of pediatric endocrinology & metabolism. 2022 ; 35( 6): 831-835.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1515/jpem-2021-0719
